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在肾切除模型中用骨形态发生蛋白-7成功治疗动力缺失性骨病

Successful treatment of an adynamic bone disorder with bone morphogenetic protein-7 in a renal ablation model.

作者信息

Lund Richard J, Davies Matthew R, Brown Alex J, Hruska Keith A

机构信息

Renal Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Am Soc Nephrol. 2004 Feb;15(2):359-69. doi: 10.1097/01.asn.0000109671.99498.08.

Abstract

An adynamic bone disorder (ABD) is an important complication of chronic kidney disease (CKD) of unknown etiology for which there is no adequate treatment. Reported is an animal model of ablative CKD complicated by an ABD characterized by the absence of secondary hyperparathyroidism and its successful treatment with a skeletal anabolic factor, bone morphogenetic protein-7 (BMP-7). Adult mice were subjected to electrocautery of the right kidney followed by left nephrectomy. Animals were randomized into groups fed normal chow or fed low-phosphate chow supplemented with calcitriol to maintain normophosphatemia in CKD. All groups were maintained on the regimens for 12 wk. Hyperphosphatemia, secondary hyperparathyroidism, and a mild osteodystrophy developed in the CKD/chow-fed group, as expected. When dietary phosphorus was restricted and calcitriol was administered in the CKD low-phosphate/calcitriol group (ABD), Ca, PO(4), and parathyroid hormone levels were maintained normal. A significant ABD developed in the ABD group characterized by significant depressions in osteoblast number, perimeters, bone formation rates, and mineral apposition rates when compared with the sham-operated, chow-fed group. The abnormal skeletal histomorphometry was reversed by BMP-7 therapy to normal values and significantly improved from the ABD group (P < 0.05). The sham-operated low-phosphate/calcitriol-fed control group and the CKD low-phosphate/calcitriol/BMP-7 groups had reduced phosphate levels compared with the other groups (P < 0.05). ABD produced in mice with CKD in the absence of hyperparathyroidism was successfully reversed with a bone anabolic, BMP-7, associated with a reduction in plasma phosphorus.

摘要

动力缺失性骨病(ABD)是慢性肾脏病(CKD)的一种重要并发症,其病因不明且尚无充分的治疗方法。本文报道了一种因切除性CKD并发ABD的动物模型,其特征为无继发性甲状旁腺功能亢进,并成功用一种骨骼合成代谢因子——骨形态发生蛋白-7(BMP-7)进行了治疗。成年小鼠接受右肾电灼术,随后进行左肾切除术。将动物随机分为两组,一组喂普通饲料,另一组喂补充骨化三醇的低磷饲料,以维持CKD小鼠的血磷正常。所有组均按这些方案维持12周。正如预期的那样,CKD/普通饲料喂养组出现了高磷血症、继发性甲状旁腺功能亢进和轻度骨营养不良。当CKD低磷/骨化三醇组(ABD组)限制饮食磷并给予骨化三醇时,钙、磷酸盐和甲状旁腺激素水平维持正常。与假手术、普通饲料喂养组相比,ABD组出现了显著的ABD,其特征为成骨细胞数量、周长、骨形成率和矿物质沉积率显著降低。BMP-7治疗使异常的骨骼组织形态计量学指标恢复到正常水平,且与ABD组相比有显著改善(P<0.05)。与其他组相比,假手术低磷/骨化三醇喂养对照组和CKD低磷/骨化三醇/BMP-7组的磷酸盐水平降低(P<0.05)。在无甲状旁腺功能亢进的情况下,CKD小鼠产生的ABD通过骨合成代谢因子BMP-7成功逆转,同时血浆磷降低。

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